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FDA 510(k) Application Details - K040306
Device Classification Name
Stimulator, Muscle, Powered
More FDA Info for this Device
510(K) Number
K040306
Device Name
Stimulator, Muscle, Powered
Applicant
BIOMEDICAL LIFE SYSTEMS, INC.
P.O. BOX 1360
VISTA, CA 92085-1360 US
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Contact
GARY BUSSETT
Other 510(k) Applications for this Contact
Regulation Number
890.5850
More FDA Info for this Regulation Number
Classification Product Code
IPF
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More FDA Info for this Product Code
Date Received
02/09/2004
Decision Date
03/23/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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